Fluid and source magma evolution of the Questa porphyry Mo deposit,New Mexico,USA

Combined fluid inclusion microthermometry and microanalysis by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) are used to constrain the hydrothermal processes forming a typical Climax-type porphyry Mo deposit. Molybdenum mineralisation at Questa occurred in two superimposed hydrothermal stages, a magmatic-hydrothermal breccia and later stockwork veining. In both stages, texturally earliest fluids were single-phase, of low salinity (~7 wt.% NaCl_equiv.) and intermediate-density. Upon decompression to ~300 bar, they boiled off a vapour phase, leaving behind a residual brine (up to 45 wt.% NaCl_equiv) at temperatures of ~420°C. The highest average Mo concentrations in this hot brine were ~500 μg/g, exceeding the Mo content of the intermediate-density input fluid by about an order of magnitude and reflecting pre-concentration of Mo by fluid phase separation prior to MoS₂ deposition from the brine. Molybdenum concentrations in brine inclusions, then, decrease down to 5 μg/g, recording Mo precipitation in response to cooling of the saline liquid to ~360°C. Molybdenite precipitation from a dense, residual and probably sulphide-depleted brine is proposed to explain the tabular shape of the ore body and the absence of Cu-Fe sulphides in contrast to the more common Cu-Mo deposits related to porphyry stocks. Cesium and Rb concentrations in the single-phase fluids of the breccia range from 2 to 8 and from 40 to 65 μg/g, respectively. In the stockwork veins, Cs and Rb concentrations are significantly higher (45–90 and 110–230 μg/g, respectively). Because Cs and Rb are incompatible and hydrothermally non-reactive elements, the systematic increase in their concentration requires two distinct pulses of fluid exsolution from a progressively more fractionated magma. By contrast, major element and ore metal concentrations of these two fluid pulses remain essentially constant. Mass balance calculations using fluid chemical data from LA-ICPMS suggest that at least 25 km³ of melt and 7 Gt of deep input fluid were necessary to provide the amount of Mo contained in the stockwork vein stage alone. While the absolute amounts of fluid and melt are uncertain, the well-constrained element ratios in the fluids together with empirical fluid/melt partition coefficients derived from the inclusion analyses suggest a high water content of the source melt of ~10%. In line with other circumstantial evidence, these results suggest that initial fluid exsolution may have occurred at a confining pressure exceeding 5 kbar. The source of the molybdenum-mineralising fluids probably was a particularly large magma chamber that crystallised and fractionated in the lower crust or at mid-crustal level, well below the shallow intrusions immediately underlying Questa and other porphyry molybdenum deposits. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

能量色散X射线荧光光谱法测定钼矿石中钼铅铁铜

建立了能量色散X射线荧光光谱法测定钼矿石中钼、铅、铁、铜的方法,讨论了粒度效应、矿物效应的影响因素,确定了采取粉末样品,用系列标准样品建立工作曲线,通过元素间相互校正消除基体效应,用内控标准样品考察了方法的精密度(RSD,n=11)为0.44%～15.4%。实际样品的测定结果和化学法相符,可满足日常分析工作需要。     

河南省栾川县罗村钼矿成矿特征及找矿

通过对河南省栾川县罗村钼矿区域地质背景、矿床地质特征与南泥湖、三道庄及东沟超大型钼矿的综合对比、分析、研究,总结归纳了矿区NWW构造形迹、小岩体与钼矿成矿关系、围岩对成矿的控制作用、围岩蚀变与成矿的关系、地球化学异常与钼矿床的关系等成矿特征.根据罗村钼矿的成矿特征,初步指出今后的找矿方向.     

酸溶——催化极谱法测定地质样品中的钨、钼

本文采用混合酸溶解样品,对影响催化体系稳定的酸度、温度和不同反应时间的因素分别进行了对比试验,确定催化体系相对稳定的最佳条件,经过大量样品的分析验证,分析方法可靠。     

商城县汤家坪钼矿地球化学特征及找矿远景

矿区地质、地球化学特征研究入手,总结了综合找矿标志,指出了进一步找矿方向。研究表明该矿床成矿组分单一,异常元素组合主要为Mo、Bi、Ag,次为W、Sn、Zn、Cu、Pb,仅有钼能形成较大规模的异常;矿床元素水平分带序列为(Mo-Bi-Ag)-(W-Sn)-(Pb-Zn-Cu),垂向分带序列为(Mo-Ag-Pb-Zn)-Cu-(Bi-W-Sn),并以w(Mo)/[w(Bi)×100]≥65,[w(Pb)×w(Zn)/w(W)×w(Sn)]≥25为判别标志,来预测深部盲矿体的存在。     

西秦岭温泉花岗岩体的新认识

温泉花岗岩体是西秦岭地区一个极具典型研究意义的复杂成因岩体和具有潜力的成矿(钼矿床)岩体。通过1：25万天水市幅区城地质调查，初步获得一些新认识：在岩体北部古坡乡-铁炉坡乡-带新发现一套蛇绿岩组合；岩体的岩石类型复杂，为一多期次侵入的复式岩体；岩体中发育大量包体，显示了岩浆混合作用的存在；另外，岩体中还发现较大体积的古老片麻岩包体和工业钼矿床。岩体主体获得259Ma的锆石U—Pb年龄。     

镍钼在黑色岩系中富集成因的实验研究

对湘西和黔北早寒武世含Ｎｉ、Ｍｏ等多金属黑色岩系进行了淋滤实验。实验分别模拟了普通雨水、富ＣＯ２气雨水及酸性雨水三种不同淋滤条件。实验表明，黑色岩系中Ｍｏ、Ｎｉ、Ｖ等元素是比较容易被淋滤出的，尤其是在酸性雨水条件下，它们的带出强度最大。本实验为镍钼富集层的成因及寻找类似的矿床提供了依据。＊据（１９６２）。图３实验样品在不同雨水淋滤条件下各个元素带出强度的比较Ｆｉｇ．３Ｃｏｍｐａｒｉｓｏｎｏｆｔｈｅｉｎｔｅｎｓｉｔｙｏｆｔｈａｔｔｈｅｖａｒｉｏｕｓｅｌｅｍｅｎｔｉｎｓａｍｐｌｅｓｉｓｌｅａｃｋｅｄｏｕｔｂｙｄｉｆｆｅｒｅｎｔｒａｉｎｗａｔｅｒｓ从图３上可以看出，不同元素的带出强度有着明显的差别。例如带出强度最大的钼与其最小的铝可以相差４～５个数量级。现代空气雨水与饱含ＣＯ２气的雨水对样品淋滤强度的图形基本相似，也就是它们对各种元素的带出强度是相似的。而酸性度很大的雨水则明显地增强了多数元素的带出强度。值得注意的是钼在上述实验的任何条件下都能被强烈的带出，这是因为在表生条件的氧化作用下，Ｍｏ４＋可氧化为Ｍｏ６＋，形成溶解度较高的钼酸或钼酸盐，在溶液中搬运或呈胶体形式迁移，而在还原条件下，在有机质及铁硫化物大量存?     

Isotope geochemistry and Re–Os geochronology of the Yanjiagou Mo deposit in the central North China Craton

The Yanjiagou deposit, located in the central North China Craton (NCC), is a newly found porphyry‐type Mo deposit. The Mo mineralization here is spatially associated with the Mapeng batholith. In this study, we identify four stages of ore formation in this deposit: pyrite phyllic stage (I), quartz–pyrite stage (II), quartz–pyrite–molybdenite stage (III), which is the main mineralization stage, and quartz–carbonate stage (IV). We present sulphur and lead isotope data on pyrite, and rhenium and osmium isotopes of molybdenite from the porphyry deposit and evaluate the timing and origin of ore formation. The δ³⁴S values of the pyrite range from ‐1.1‰ to −0.6‰, with an average of −0.875‰, suggesting origin from a mixture of magmatic/mantle sources and the basement rocks. The Pb isotope compositions of the pyrite show a range of 16.369 to 17.079 for ²⁰⁶Pb/²⁰⁴Pb, 15.201 to 15.355 for ²⁰⁷Pb/²⁰⁴Pb, and 36.696 to 37.380 for ²⁰⁸Pb/²⁰⁴Pb, indicating that the ore‐forming materials were derived from a mixture of lower crust (or basement rocks) and mantle. Rhenium contents in molybdenite samples from the main ore stage are between 74.73 to 254.43 ppm, with an average of 147.9 ppm, indicating a mixed crustal‐mantle source for the metal. Eight molybdenite separates yield model ages ranging from 124.17 to 130.80 Ma and a mean model age of 128.46 Ma. An isochron age of 126.7 ± 1.1 Ma (MSWD = 2.1, initial ¹⁸⁷Os = 0.0032 ± 0.0012 ppb) is computed, which reveals a close link between the Mo mineralization and the magmatism that generated the Mapeng batholith. The age is close to the zircon U–Pb age of ca. 130 Ma from the batholith reported in a recent study. The age is also consistent with the timing of mineralization in the Fuping ore cluster in the central NCC, as well as the peak time of lithosphere thinning and destruction of the NCC. We evaluate the spatio‐temporal distribution of the Mo deposits in the NCC and identify three important molybdenum provinces along the northern and southern margins of the craton formed during three distinct episodes: Middle to Late Triassic (240–220 Ma), Early Jurassic (190–175 Ma), and Late Jurassic to Early Cretaceous (150–125 Ma). The third period is considered to mark the most important metallogenic event, coinciding with the peak of lithosphere thinning and craton destruction in the NCC. Copyright © 2014 John Wiley & Sons, Ltd.     

浙江省青田县石平川钼矿床新发现及找矿前景

长期以来,石平川钼矿床一直被认为是典型的石英脉型矿床,矿体分布于石平川岩体内外接触带上下100m以内。经过近年的地质工作发现,距石平川岩体外接触带400m~500m的侏罗系西山头组第二岩性段地层中存在细脉型辉钼矿体,从而形成下部大脉型石英辉钼矿体、上部细脉型辉钼矿体的二元结构。这一发现为开展深部及外围找矿,扩大资源储量规模提供了新的前景。     

内蒙古二连—东乌旗铜钼多金属成矿带中西段 找矿进展

二连—东乌旗成矿带位于西伯利亚板块和华北板块之间的兴蒙造山带东段,属西伯利亚板块东南南大陆边缘早古生代火山岛弧带、晚古生代二连－贺根山板块对接带。自中生代开始,区内逐渐向滨太平洋构造域发展过渡,并在中生代晚期经历了明显的由挤压构造体系向伸展构造体系的转换过程,在一系列构造演化及其相应的岩浆作用、火山作用和变质作用过程中,分别伴随着金、钼、铜、铅、锌等多金属富集和矿化,该地区具有优越的成矿条件。